A Pulse–chase EdU Method for Detection of Cell Division Orientation in Arabidopsis and Juncus prismatocarpus Leaf Primordia

Materials and Reagents

1. 1.5- or 5-ml tube

2. APS-coated glass slide (Matsunami, catalog number: SAPS )

3. Coverslip (Matsunami, catalog number: C025601 )

4. Razor blade

5. Aluminum foil

6. Gloves

7. Arabidopsis seed

8. J. prismatocarpus seed

9. 10x phosphate buffered saline (PBS) (pH 7.4) (Nacalai Tesque, catalog number: 27575-31 ) (store at room temperature)

10. 0.5% (v/v) Triton X-100 in 1x PBS (pH 7.4) (store at room temperature)

11. Click-iT^TM EdU Cell Proliferation Kit for Imaging (Thermo Fisher Scientific, catalog number: C10337 ) (store at 4 °C and protect unopened components from light; store stock and working solutions following the manufacturer’s specifications)

12. DAPI (Thermo Fisher Scientific, catalog number: D1306 ) (store at 4 °C and protect from light)

13. Höechst 33342 (Component G of 11)

14. Ethanol (Wako, catalog number: 057-00451 )

15. Ethanol series (30%, 50%, 70%, 90%, and 100%) (store at room temperature)

16. Xylene (Wako, catalog number: 244-00081) (store at room temperature, preferably in a fume hood)

17. (Optional) Histo-Clear (National Diagnostics, catalog number: HS-200 )

18. Paraffin (McCormick Scientific, catalog number: 39502004 ) (store at room temperature and avoid moisture)

19. Distilled water (dH₂O)

20. Sucrose (Nacalai Tesque, catalog number: 30403-55 )

21. Vitamin B5 (Wako ASB-00022727-001 )

22. Agar (Wako, catalog number: 016-11875 )

23. 1 M KOH

24. Formaldehyde (Wako, catalog number: 064-00406 )

25. Glacial acetic acid (Wako, catalog number: 017-00251 )

26. Murashige and Skoog (MS) plant salt mixture (Wako, catalog number: 392-00591 )

27. MS plates and liquid MS medium (see Recipes) (store at 4°C)

28. EdU detection cocktail (see Recipes)

29. FAA (see Recipes) (store at room temperature)

Equipment

1. Forceps

2. Shaker (AS ONE, model: SRR-2 )

3. Confocal laser scanning microscope (Zeiss, model: LSM 780 )

4. Incubator (Taitec, model: HB-80 )

5. Paraffin mold (multiple)

6. Rotary microtome (Leica, model: Microm HM 355S )

7. Slide warmer (Tissue Tek, model: PS-52S )

8. Slide holder

9. Glass tank (multiple)

Software

1. Zen 2012 blue edition

Procedure

1. Arabidopsis leaf primordia

   1. Germinate surface-sterilized Arabidopsis seeds on MS plates. At six days after sowing (DAS) at 22 °C under continuous light (70 μmol·m^-2·sec^-1 from white florescent lamps), select healthy seedlings and cut the root and part of the hypocotyl (Figure 1) using a razor blade.

      
      

      
      Figure 1. Uncut (left) and cut (right) Arabidopsis samples. Scale bar = 1 mm.

      
      

   2. Transfer samples to a 1.5- or 5-ml tube approximately half-filled with liquid MS medium containing 10 μM EdU. Incubate for 45 min under continuous light at room temperature.

   3. Transfer samples to a new tube filled with liquid MS medium without EdU. Gently shake [≤ 50 revolutions per minute (rpm)] for 5 min, three times.

   4. Incubate samples in liquid MS medium for 6 h 45 min under continuous light at room temperature. The total chase time is 7 h, including the wash in Step A3.

   5. Transfer samples to a new tube filled with FAA to fix the samples overnight at 4 °C. Degas by vacuum infiltration a few times until the samples sink. Alternatively, briefly centrifuge (130 x g, 5 s) to enhance fixation.

   6. (Optional) Incubate samples in 90% acetone on ice for 10 min.

   7. Shake (100 rpm) samples in 0.5% (v/v) Triton X-100 in 1x PBS (pH 7.4) for 5 min, two times.

   8. Shake (100 rpm) samples in 1x PBS (pH 7.4) for 5 min, two times.

   9. Prepare EdU detection cocktail (see Recipes) in a new tube. Transfer samples to it and incubate for 30 min in the dark.

   10. Transfer samples to a new tube filled with 1x PBS (pH 7.4) and shake (100 rpm) for 5 min, three times.

   11. Transfer samples to a new tube filled with 1x PBS (pH 7.4) containing 1 μg/ml DAPI and incubate for 30 min in the dark.

   12. Shake (100 rpm) samples in 1x PBS (pH 7.4) for 20 min, two times and a third time overnight.

   13. Mount samples with 1x PBS (pH 7.4) on a slide and observe the first pair of leaf primordia using a confocal laser scanning microscope equipped with a 40x oil immersion objective. Use a 488 nm laser to excite Alexa 488 (now covalently bonded to EdU) and a 490-535 nm emission spectrum to detect Alexa 488. Use a 405 nm laser to excite DAPI and a 420-470 nm emission spectrum to detect DAPI.

   14. Store samples in 1x PBS (pH 7.4) in the dark at 4 °C for up to 6 months.




2. Juncus prismatocarpus leaf primordia

   1. Germinate surface-sterilized J. prismatocarpus seeds on MS plates. At 28 DAS at 22 °C under continuous light (70 μmol·m^-2·sec^-1 from white florescent lamps), select healthy seedlings and cut the upper parts of leaves and elongated roots (Figure 2) using a razor blade.

      
      

      
      Figure 2. Uncut (left) and cut (right) Juncus prismatocarpus samples. Scale bar = 5 mm.

   
   

   2. Transfer samples to a 1.5- or 5-ml tube approximately half-filled with liquid MS medium containing 10 μM EdU. Incubate for 2 h under continuous light at room temperature.

   3. Transfer samples to a new tube filled with liquid MS medium without EdU. Gently shake (≤ 50 rpm) for 5 min, three times.

   4. Incubate samples in liquid MS medium for 13 h 15 min under continuous light at room temperature. The total chase time is 13.5 h, including the wash in Step B3.

   5. Transfer samples to a new tube filled with FAA to fix samples overnight at 4 °C. Degas by vacuum infiltration for a few times until the samples sink.

   6. Dehydrate samples through an increasing series of ethanol concentrations, including 50%, 70%, 90%, and three changes of 100% ethanol. Incubate samples in each solution for 1 h.

   7. Replace ethanol with xylene through an increasing series of xylene/ethanol concentrations, including 25%, 50%, 75%, and three changes of 100% xylene. Incubate samples in each solution for 30 min.

   8. Infiltrate samples with paraffin through an increasing series of paraffin/xylene concentrations at 60 °C, including 25%, 50%, 75%, and 100% paraffin. Incubate samples in 25% paraffin/xylene overnight, in 50% and 75% paraffin/xylene for 4 h on the second day, and in 100% paraffin during the second overnight.

   9. Incubate samples in paraffin for three additional days at 60 °C. Replace the 100% paraffin three times per day at a minimum interval of 4 h.

   10. Embed samples in the desired orientation in a mold by solidifying the paraffin at room temperature or placing the mold on ice.

   11. Section samples (8 μm) using a rotary microtome. Add dH₂O on top of a glass slide until dH₂O covers its entire surface. Mount serial sections on dH₂O. Heat the slide on a slide warmer at 42 °C overnight.

   12. Place slides (now containing sectioned samples) on a slide holder. Clear the paraffin by allowing the slide holder to pass through glass tanks containing the following in order: 100% xylene for 10 min, two times; 50% xylene/ethanol for 5 min; and 100% ethanol for 5 min.

   13. Rehydrate samples by allowing the slide holder to pass through glass tanks containing the following in order: 90%, 70%, 50%, and 30% ethanol for 1 min each; dH₂O for 5 min, two times; and 1x PBS (pH 7.4) for 5 min, two times.

   14. Briefly remove the liquid from the slides and apply 300 μl freshly prepared EdU detection cocktail to each slide using a pipette. Gently cover the slide with a coverslip and incubate for 30 min in the dark.

   15. Briefly remove the liquid from the slides and place the slides on a slide holder. Wash samples by allowing the slide holder to pass through glass tanks containing 1x PBS (pH 7.4) for 5 min, three times.

   16. Briefly remove the liquid from the slides and apply 300 μl 1x PBS (pH 7.4) containing 8 μg/ml Höechst 33342 to each slide using a pipette. Gently cover the slide with a coverslip and incubate for 30 min in the dark.

   17. Briefly remove the liquid from the slides and place them on a slide holder. Wash samples by allowing the slide holder to pass through glass tanks containing 1x PBS (pH 7.4) for 20 min, two times, then a third time overnight.

   18. Apply 300 μl 1x PBS (pH 7.4) to the slides and gently cover each slide with a coverslip. Observe the sectioned samples using a confocal laser scanning microscope equipped with a 40x oil immersion objective. Use a 488 nm laser to excite Alexa 488 (now covalently bonded to EdU) and a 490-535 nm emission spectrum to detect Alexa 488. Use a 405 nm laser to excite Höechst 33342 and a 420-470 nm emission spectrum to detect Höechst 33342.

   19. Store slides in a desiccated slide box at 4 °C for up to 6 months.

Data analysis

Cell pairs suitable for cell division orientation analysis are easily recognized in both Arabidopsis (Figure 3A) and J. prismatocarpus (Figure 3B) (Yin and Tsukaya, 2016 and 2019). Using these cell pairs, cell division angles can be quantified (Figure 4). The cell division angles are further categorized according to their values. In Arabidopsis, the cell division angles are categorized as follows: along the proximal-distal axis (0-30° and 150-180°), perpendicular to the proximal-distal axis (60-90° and 90-120°), and intermediate (30-60° and 120-150°). In J. prismatocarpus, the cell division angles are categorized as follows: along the thickness orientation (0-30° and 150-180°), perpendicular to the thickness orientation (60-90° and 90-120°), and intermediate (30-60° and 120-150°). From 1620 cell pairs (three samples) of Arabidopsis, leaf primordia were determined to be marked by non-stochastic cell division orientations in different localized regions (Yin and Tsukaya, 2016). From 379 cell pairs (26 samples) of J. prismatocarpus abaxialized leaf blades (Yamaguchi et al., 2010), cell divisions were found to be more frequent in the leaf thickness orientation and distributed towards the shoot apical meristem (Yin and Tsukaya, 2019).

Notes

1. Preserve the cut root as a positive control, because cells in the root apical meristem are easily stained by EdU.

2. To ensure accurate timing when incubating many samples, add EdU to the liquid MS medium after all samples have been transferred into the tube.

3. If the overall EdU (Alexa 488) signal is low, the following can be performed: cut the hypocotyl at a position near the shoot apex, remove older leaves, and increase the pulse time in Steps A2 and B2.

4. If EdU (Alexa 488) pairs are not abundant, the following can be performed: increase the chase time in Steps A4 and B4.

5. When working on a new species, the pulse and chase times must be determined empirically; the times of Arabidopsis and J. prismatocarpus can be used as references. The pulse time can be determined by gradually increasing the EdU incubation time in Steps A2 and B2 until the overall EdU (Alexa 488) signal reaches a satisfactory level. The chase time can be determined by gradually increasing the chase time in 1-h increments in Steps A4 and B4 until there are sufficient EdU (Alexa 488) pairs for quantitative analysis.

6. The EdU detection cocktail must be made in the order of components shown in the Recipes section; it must be made fresh each time, immediately prior to detection.

7. Keep samples and slides in the dark (e.g., wrapped in aluminum foil) following detection by the EdU detection cocktail.

8. Xylene is toxic, flammable, and highly volatile. It must be handled with great care in a fume hood. Alternatives such as Histo-Clear can be used as a safe replacement for xylene.

9. When handling xylene, paraffin, DAPI, and Höechst 33342, gloves must be worn.

10. When applying a coverslip to a slide, take care not to generate bubbles on or near sections.

Recipes

1. MS plates

   MS plant salt mixture                                             1 bag (~4.6 g)

   Sucrose (2%, w/v)                                                    20 g

   Vitamin B5                                                               1 ml

   Agar (4%, w/v)                                                         40 g

   Dissolve the above in ~800 ml dH₂O, adjust pH to ~5.8 using 1 M KOH, add dH₂O to a final volume of 1,000 ml, autoclave, and allow to cool in plates

2. Liquid MS medium

   Prepare in the same manner shown above for MS plates, but omit the use of agar

3. FAA

   Formaldehyde                                        50 ml           

   Glacial acetic acid                                  25 ml

   Ethanol                                                   250 ml

   dH₂O                                                       175 ml

4. EdU detection cocktail [made from Click-iT^TM EdU Cell Proliferation Kit for Imaging, and must be prepared in the following order (indicated by numbering for clarity)]

   a. Click-iT^TM EdU reaction buffer (diluted from Component D with dH₂O)                                         215 μl

   b. CuSO₄ aqueous solution (Component E)                                                                                           10 μl

   c. Alexa Fluor^® 488 (mix Component B and Component C)                                                                 0.6 μl

   d. Reaction buffer additive (diluted from Component F)                                                                      25 μl

Acknowledgments

We thank Professors Akihiko Nakano (The University of Tokyo, Japan) and Takashi Ueda (The University of Tokyo, Japan), for their permission to use the confocal microscope. This work was supported by the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan (Scientific Research on Priority Areas and Scientific Research on Innovative Areas, grants no. 25113001, 25113002, and 19H05672) and the Japan Society for the Promotion of Science Postdoctoral Fellowship for Research in Japan (grant no. P19085).

Competing interests

There are no competing interests.

References

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